FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BIVONA NASAL TURBINATE STENT

K Number: K935053 · Decision Jul 1, 1994
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
45
Applicant Total
50
Review Days
253

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Basic Information

Device Name
BIVONA NASAL TURBINATE STENT
K Number
K935053
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4780
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bivona Medical Technologies
Date Received
October 21, 1993
Decision Date
July 1, 1994
Product Code
LYA
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LYA Splint, Intranasal Septal

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Other Clearances by Bivona Medical Technologies

K Number Device Name
K952700 SUPERSLICK
K942025 BURGET NASAL STENT
K944178 BIVONA FLEXTEND PEDIATRIC & NEONATAL TRACHEOSTROMY TUBES
K933398 BIVONA ILLUMINATED ENDOTRACHEAL TUBE
K931749 BIVONA(R) ICU ENDOTRACHEAL TUBE
K922665 BIVONA HYPERFLEX TRACHEOSTOMY TUBE
K923878 BIVONA CUSTOMIZED TRACHEOSTOMY TUBES
K920604 BIVONA TRACHEAL T-TUBE STENT
K915761 BIVONA-COLORADO VOICE PROSTHESIS
K915799 BIVONA SLEEP APNEA TUBE
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